Results 21 to 30 of about 346,856 (231)

Juvenile dermatomyositis and nephrotic syndrome: A case report and a mini literature review

open access: yesFrontiers in Pediatrics, 2023
BackgroundRenal involvement is rarely reported in juvenile dermatomyositis and may be caused by the toxic effects of myoglobinuria or an autoimmune reaction. We report a case of dermatomyositis and nephrotic syndrome in a child to explore the association
Weiran Zhou   +4 more
doaj   +1 more source

JAK inhibitors are effective in a subset of patients with juvenile dermatomyositis: a monocentric retrospective study.

open access: yesRheumatology, 2021
OBJECTIVE To evaluate the efficacy and safety of JAK inhibitors (JAKi) in juvenile dermatomyositis (JDM). METHODS We conducted a single-center retrospective study of patients with JDM treated by JAKi with a follow-up of at least 6 months. Proportion of
Tom Le Voyer   +14 more
semanticscholar   +1 more source

An 8-year-old-girl with juvenile dermatomyositis and autoimmune thyroiditis in Tanzania: a case report

open access: yesJournal of Medical Case Reports, 2021
Background Juvenile dermatomyositis is an inflammatory disease of muscles, skin, and blood vessels of unknown cause affecting all age and ethnic groups, with a reported incidence of 1.9–4.1 per million.
Fatima Mussa   +2 more
doaj   +1 more source

Juvenile dermatomyositis. Where are we now?

open access: yesClinical and Experimental Rheumatology, 2022
Juvenile onset idiopathic inflammatory myopathy (IIM) has many similarities and distinct differences from adult-onset disease. This review will focus on recent developments in understanding and treatment of juvenile dermatomyositis (JDM), the most common
L. McCann   +3 more
semanticscholar   +1 more source

Role of CD14+ monocyte-derived oxidised mitochondrial DNA in the inflammatory interferon type 1 signature in juvenile dermatomyositis

open access: yesAnnals of the Rheumatic Diseases, 2022
Objectives To define the host mechanisms contributing to the pathological interferon (IFN) type 1 signature in Juvenile dermatomyositis (JDM). Methods RNA-sequencing was performed on CD4+, CD8+, CD14+ and CD19+ cells sorted from pretreatment and on ...
M. Wilkinson   +14 more
semanticscholar   +1 more source

Erythroderma as a presenting sign of juvenile overlap syndrome

open access: yesIndian Journal of Paediatric Dermatology, 2023
Juvenile dermatomyositis (JDM), which is rarely presented with erythroderma, and juvenile morphea are both autoimmune connective tissue diseases. We report a 14-year-old male child with resistant generalized erythroderma and mild proximal muscle weakness
Sarah Hamdy Soliman   +5 more
doaj   +1 more source

Banker Type of Juvenile Dermatomyositis

open access: yesIndian Journal of Dermatology
Sunil K. Gupta, Ratnakar Shukla
doaj   +2 more sources

Short-term effectiveness of baricitinib in children with refractory and/or severe juvenile dermatomyositis

open access: yesFrontiers in Pediatrics, 2022
Objective To determine the short-term effectiveness safety of baricitinib in children with refractory and/or severe juvenile dermatomyositis (rsJDM) in a real-world setting. Methods This was a single-center retrospective study, including 20 children with
Zhaoling Wang   +8 more
semanticscholar   +1 more source

Juvenile Dermatomyositis: New Clues to Diagnosis and Therapy

open access: yesCurrent Treatment Options in Rheumatology, 2021
To identify clues to disease activity and discuss therapy options. The diagnostic evaluation includes documenting symmetrical proximal muscle damage by exam and MRI, as well as elevated muscle enzymes—aldolase, creatine phosphokinase, LDH, and SGOT—which
L. Pachman   +3 more
semanticscholar   +1 more source

Case of a fatal lung disease in a child with juvenile dermatomyositis

open access: yesZdorovʹe Rebenka, 2017
The article presents a case of a fatal lung disease in a child with juvenile dermatomyositis. Juvenile dermatomyositis is a serious disease with an unpredictable course, and lung damage in juvenile dermatomyositis is one of the most severe manifestations
O.A. Oshlianska   +5 more
doaj   +1 more source

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